V17G (p.Val17Gly) variant of CASP9 (Caspase-9)
V17G (p.Val17Gly) in CASP9 (Caspase-9) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.48 / 1. The record also includes population frequency data and structural context.
V17G (p.Val17Gly) variant details
- p.Val17Gly
- cosmic curated COSV61600
- ExAC rs766813971
- gnomAD rs766813971
- Missense
- Variant Prioritization Score for Impact Estimate 0.48
- REVEL 0.37
- CADD 26.10
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the 1KG:MSL population (allele frequency 0.013)
- Structural context available